Disease #05587 (FAME3;FMCTE3 (epilepsy, myoclonic, familial adult, type 3 (FAME3, FMCTE3)), OMIM:613608)

Official abbreviation	FAME3;FMCTE3
Name	epilepsy, myoclonic, familial adult, type 3 (FAME3, FMCTE3)
OMIM ID	613608
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	MARCH6
Associated tissues	-
Disease features	autosomal dominant
Remarks	-
Date created	2019-04-10 21:07:01 +02:00 (CEST)
Date last edited	2019-12-19 19:06:19 +01:00 (CET)

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Global Variome shared LOVD